ClinVar Miner

List of variants reported as uncertain significance for hereditary diffuse gastric adenocarcinoma by Illumina Laboratory Services, Illumina

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 46
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004360.5(CDH1):c.*424T>A rs867174076 0.00056
NM_004360.5(CDH1):c.*346A>T rs754600872 0.00045
NM_004360.5(CDH1):c.*623A>G rs142125691 0.00034
NM_004360.5(CDH1):c.*1872C>T rs545034372 0.00022
NM_004360.5(CDH1):c.33G>C (p.Leu11=) rs730881654 0.00022
NM_004360.5(CDH1):c.*196T>G rs576484193 0.00021
NM_004360.5(CDH1):c.*1545T>C rs186584057 0.00011
NM_004360.5(CDH1):c.2512A>G (p.Ser838Gly) rs121964872 0.00011
NM_004360.5(CDH1):c.*1076T>C rs541517386 0.00006
NM_004360.5(CDH1):c.*192C>T rs576309125 0.00006
NM_004360.5(CDH1):c.*575A>C rs886052242 0.00006
NM_004360.5(CDH1):c.*615G>A rs148655354 0.00006
NM_004360.5(CDH1):c.*959C>A rs886052243 0.00006
NM_004360.5(CDH1):c.*1049A>C rs886052244 0.00004
NM_004360.5(CDH1):c.*1285T>C rs369689471 0.00004
NM_004360.5(CDH1):c.*193G>C rs886052238 0.00004
NM_004360.5(CDH1):c.-41C>A rs730881658 0.00004
NM_004360.5(CDH1):c.*409T>A rs778711236 0.00003
NM_004360.5(CDH1):c.*1435A>T rs886052245 0.00002
NM_004360.5(CDH1):c.*582C>A rs920956371 0.00002
NM_004360.5(CDH1):c.*172A>C rs886052237 0.00001
NM_004360.5(CDH1):c.*1765A>G rs1343770513 0.00001
NM_004360.5(CDH1):c.1315G>A (p.Ala439Thr) rs758764445 0.00001
NM_004360.5(CDH1):c.150C>A (p.Arg50=) rs786201262 0.00001
NM_004360.5(CDH1):c.1843A>G (p.Ile615Val) rs1003012321 0.00001
NM_004360.5(CDH1):c.2219C>A (p.Pro740His) rs730881669 0.00001
NM_004360.5(CDH1):c.2505T>C (p.Tyr835=) rs786202613 0.00001
NM_004360.5(CDH1):c.370C>T (p.Arg124Cys) rs748086082 0.00001
NM_004360.5(CDH1):c.462A>G (p.Arg154=) rs1057520261 0.00001
NM_004360.5(CDH1):c.794A>T (p.Glu265Val) rs587782728 0.00001
NM_004360.5(CDH1):c.*1591T>C rs886052246
NM_004360.5(CDH1):c.*221del rs145920869
NM_004360.5(CDH1):c.*221dup rs145920869
NM_004360.5(CDH1):c.*236C>T rs1961559604
NM_004360.5(CDH1):c.*309C>T rs562205897
NM_004360.5(CDH1):c.*474_*475dup rs113202135
NM_004360.5(CDH1):c.*475del rs113202135
NM_004360.5(CDH1):c.*627T>G rs1567518268
NM_004360.5(CDH1):c.1018A>T (p.Thr340Ser) rs116093741
NM_004360.5(CDH1):c.1137+9A>T rs780705655
NM_004360.5(CDH1):c.1170C>T (p.Asn390=) rs766505270
NM_004360.5(CDH1):c.1360G>C (p.Val454Leu) rs587780112
NM_004360.5(CDH1):c.1366G>T (p.Val456Leu) rs974965262
NM_004360.5(CDH1):c.1716T>C (p.Ser572=) rs876660176
NM_004360.5(CDH1):c.1887A>G (p.Glu629=) rs886052236
NM_004360.5(CDH1):c.597A>G (p.Thr199=) rs1960738532

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.